Yuan Xiaoya, Zhou Chou, Jin Yanrong, Jing Qiuye, Yang Yaling, Shen Xu, Tang Qi, Mu Yuanhua, Du An-Ke
College of Materials Science and Engineering, Chongqing Jiaotong University, Chongqing 400074, China.
College of Materials Science and Engineering, Chongqing Jiaotong University, Chongqing 400074, China.
J Colloid Interface Sci. 2016 Apr 15;468:211-219. doi: 10.1016/j.jcis.2016.01.048. Epub 2016 Jan 22.
3D porous framework composed of exfoliated ultrathin nanosheets is a hot topic in the field of energy storage and conversion. A facile method to prepare 3D mesoporous C3N4 with few-layered nanosheets interconnected in large quantity via H2SO4 intercalation and subsequent thermal treatment was described herein. The obtained thermally-exfoliated C3N4 (TE-C3N4) was thoroughly characterized by scanning electron microscopy (SEM), high-resolution transmission electron microscopy (HRTEM), powder X-ray diffraction (XRD), X-ray photoelectron spectroscopy (XPS), Fourier transform infrared (FTIR) spectroscopy, atomic force microscopy (AFM), UV-Vis diffuse reflectance spectroscopy (DRS) and Brunauer-Emmett-Teller (BET) measurements. The detailed analysis indicated that TE-C3N4 possessed enlarged inter-layer space, enhanced UV-light adsorption and high specific surface area with 3D interconnected structure composed of ultrathin 2D nanosheets. Compared to bulk C3N4, TE-C3N4 showed an enhanced photocatalytic activity for photodegradation of Rhodamine B under UV-light irradiation and exhibited no significant loss of photocatalytic activity after 11 recycled runs. The pseudo-first reaction rate constant for TE-C3N4 was about four times higher than that for pure bulk-C3N4. The better photocatalytic performance could be attributed to more active catalytic sites, prolonged photo-excited carrier lifetime and shorted pathway of the carriers to the reaction sites.
由剥离的超薄纳米片组成的三维多孔框架是储能与转换领域的一个热门话题。本文描述了一种通过硫酸插层及后续热处理制备具有大量相互连接的少层纳米片的三维介孔氮化碳的简便方法。通过扫描电子显微镜(SEM)、高分辨率透射电子显微镜(HRTEM)、粉末X射线衍射(XRD)、X射线光电子能谱(XPS)、傅里叶变换红外(FTIR)光谱、原子力显微镜(AFM)、紫外-可见漫反射光谱(DRS)和布鲁诺尔-埃米特-泰勒(BET)测量对所得的热剥离氮化碳(TE-C3N4)进行了全面表征。详细分析表明,TE-C3N4具有扩大的层间空间、增强的紫外光吸附以及由超薄二维纳米片组成的三维互连结构的高比表面积。与块状氮化碳相比,TE-C3N4在紫外光照射下对罗丹明B的光降解表现出增强的光催化活性,并且在11次循环运行后光催化活性没有显著损失。TE-C3N4的准一级反应速率常数约为纯块状氮化碳的四倍。更好的光催化性能可归因于更多的活性催化位点、延长的光激发载流子寿命以及载流子到反应位点的更短路径。